| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:18084070-18084530 | Common:8; Rare:266; Clinvar:8; Clinvar (benign):4 | ||||
| chr8:18084740-18085200 | Common:5; Rare:200; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr8:19313563-19314074 | Common:11; Rare:265 | ||||
| chr8:19757050-19757530 | Common:8; Rare:217 | ||||
| chr8:19757510-19757640 | Common:3; Rare:26 | ||||
| chr8:19757808-19757992 | Common:3; Rare:36 | ||||
| chr8:19758017-19758120 | Rare:14 | ||||
| chr8:19816999-19817651 | Common:18; Rare:399 | ||||
| chr8:20197227-20197421 | Common:2; Rare:174 | ||||
| chr8:21919512-21919776 | Common:4; Rare:206 | ||||
| chr8:22048838-22049087 | Common:6; Rare:88 | ||||
| chr8:22089085-22089265 | Rare:113 | ||||
| chr8:22089460-22089800 | Common:4; Rare:159 | ||||
| chr8:22109359-22109613 | Common:11; Rare:174 | ||||
| chr8:22131010-22131510 | Common:3; Rare:197 |